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The iodine catalysed bromination of some aromatic compounds

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dc.contributor.authorSimmers, Mary Glen
dc.date.accessioned2011-12-13T21:28:51Z
dc.date.accessioned2022-10-31T22:00:07Z
dc.date.available2011-12-13T21:28:51Z
dc.date.available2022-10-31T22:00:07Z
dc.date.copyright1941
dc.date.issued1941
dc.description.abstractLucas (Lucas, J.A.C.S., 1925, 2475) first suggested that electron displacement might influence halogen addition, and Burton and Ingold (Burton and Ingold, J.C.S., 1928, 1894) first formulated an orientation theory for conjugative addition. After this, knowledge concerning the mechanisms of organic halogenations developed rapidly, and by 1931, Ingold and Ingold (Ingold and Ingold, J.C.S., 1931, 2359) were able to put forward a general theory of the mechanism of halogen addition to compounds containing an ethylene link.en_NZ
dc.formatpdfen_NZ
dc.identifier.urihttps://ir.wgtn.ac.nz/handle/123456789/27169
dc.languageen_NZ
dc.language.isoen_NZ
dc.publisherTe Herenga Waka—Victoria University of Wellingtonen_NZ
dc.rights.holderAll rights, except those explicitly waived, are held by the Authoren_NZ
dc.rights.licenseAuthor Retains Copyrighten_NZ
dc.rights.urihttps://www.wgtn.ac.nz/library/about-us/policies-and-strategies/copyright-for-the-researcharchive
dc.subjectChemistryen_NZ
dc.titleThe iodine catalysed bromination of some aromatic compoundsen_NZ
dc.typeTexten_NZ
thesis.degree.disciplineChemistryen_NZ
thesis.degree.grantorTe Herenga Waka—Victoria University of Wellingtonen_NZ
thesis.degree.levelMastersen_NZ
thesis.degree.nameMaster of Scienceen_NZ
vuwschema.type.vuwAwarded Research Masters Thesisen_NZ

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